3206-31-3 Usage
Uses
Used in Chemical and Industrial Applications:
Triethyl nitrilotricarboxylate is used as a chelating agent for its ability to bind metal ions, which is crucial in preventing unwanted deposits and precipitation in chemical processes.
Used in Metal Cleaning Products:
In the metal cleaning industry, triethyl nitrilotricarboxylate is used as an active ingredient to facilitate the removal of metal ions, ensuring the effectiveness of cleaning solutions.
Used in Metal Plating Solutions:
Triethyl nitrilotricarboxylate is utilized as a chelating agent in metal plating solutions to improve the quality and uniformity of the plating process by managing the metal ion activity.
Used as a Corrosion Inhibitor in Industrial Water Treatment:
In industrial water treatment, triethyl nitrilotricarboxylate serves as a corrosion inhibitor, protecting metal surfaces from corrosion by sequestering metal ions that could otherwise cause damage.
Used in Pharmaceutical Production:
Triethyl nitrilotricarboxylate is employed in the production of pharmaceuticals, where its chelating properties are beneficial for the synthesis of certain drugs or as a component in formulations.
Used as a Complexing Agent in Analytical Chemistry:
In analytical chemistry, triethyl nitrilotricarboxylate is used as a complexing agent to help in the analysis of metal ions, enhancing the accuracy and efficiency of various analytical techniques.
Check Digit Verification of cas no
The CAS Registry Mumber 3206-31-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,0 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3206-31:
(6*3)+(5*2)+(4*0)+(3*6)+(2*3)+(1*1)=53
53 % 10 = 3
So 3206-31-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H15NO6/c1-4-14-7(11)10(8(12)15-5-2)9(13)16-6-3/h4-6H2,1-3H3
3206-31-3Relevant academic research and scientific papers
Heterocyclic Polyfluoro-compounds. Part 40. Preparation of Polyfluoroazepines
Barlow, Michael G.,Harrison, Geoffrey M.,Haszeldine, Robert N.,Morton, William D.,Shaw-Luckman, Peter,Ward, Mavis D.
, p. 2101 - 2104 (2007/10/02)
The hexafluoro-Dewar-benzene adduct of phenyl azide yields hexafluoro-1-phenyl-1H-azepine on pyrolysis.Reaction of ethyl azidoformate with hexafluorobenzene yields ethyl hexafluoro-1H-azepine-1-carboxylate (21percent), with octafluoronaphthalene yields 1,2-(ethoxycarbonylimino)-1,2,3,4,5,6,7,8-octafluoro-1,2-dihydronaphthalene (23percent), and with 1,2,3,4-tetrafluoronaphthalene yields 1,2-(ethoxycarbonylimino)-1,2,3,4-tetrafluoro-1-12-dihydronaphthalene (18percent) and ethyl 5,6,7,8-tetrafluoro-1-naphthylcarbamate (48percent).No azepines were obtained from the reaction of cyanogen azide with the two naphthalenes.
